Identification of recurrent type-2 NF1 microdeletions reveals a mitotic nonallelic homologous recombination hotspot underlying a human genomic disorder

Vogt, J., Mussotter, T., Bengesser, K., Claes, K., Högel, J., Chuzhanova, N. ORCID: 0000-0002-4655-3618, Fu, C., Van den Ende, J., Mautner, V.F., Cooper, D.N., Messiaen, L. and Kehrer-Sawatzki, H., 2012. Identification of recurrent type-2 NF1 microdeletions reveals a mitotic nonallelic homologous recombination hotspot underlying a human genomic disorder. Human Mutation, 33 (11), pp. 1599-1609.

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Item Type:	Journal article
Publication Title:	Human Mutation
Creators:	Vogt, J., Mussotter, T., Bengesser, K., Claes, K., Högel, J., Chuzhanova, N., Fu, C., Van den Ende, J., Mautner, V.F., Cooper, D.N., Messiaen, L. and Kehrer-Sawatzki, H.
Date:	2012
Volume:	33
Number:	11
Divisions:	Schools > School of Science and Technology
Record created by:	EPrints Services
Date Added:	09 Oct 2015 10:20
Last Modified:	09 Jun 2017 13:26
URI:	https://irep.ntu.ac.uk/id/eprint/11507

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